rs154774640
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs154774640(C;G) |
| Make rs154774640(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 15 |
| Position | 68218584 |
| Gene | CLN6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs154774640 |
| dbSNP (classic) | rs154774640 |
| ClinGen | rs154774640 |
| ebi | rs154774640 |
| HLI | rs154774640 |
| Exac | rs154774640 |
| Gnomad | rs154774640 |
| Varsome | rs154774640 |
| LitVar | rs154774640 |
| Map | rs154774640 |
| PheGenI | rs154774640 |
| Biobank | rs154774640 |
| 1000 genomes | rs154774640 |
| hgdp | rs154774640 |
| ensembl | rs154774640 |
| geneview | rs154774640 |
| scholar | rs154774640 |
| rs154774640 | |
| pharmgkb | rs154774640 |
| gwascentral | rs154774640 |
| openSNP | rs154774640 |
| 23andMe | rs154774640 |
| SNPshot | rs154774640 |
| SNPdbe | rs154774640 |
| MSV3d | rs154774640 |
| GWAS Ctlg | rs154774640 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs154774640(G;G) |
| Alt | rs154774640(G;G) |
| Reference | Rs154774640(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | CLN6 |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000015.9:g.68510922G>C |
| CLNSRC | |
| CLNACC | RCV000058908.1, |
